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双泛素(Ubd)是大鼠病毒触发自身免疫性糖尿病的易感基因。

Diubiquitin (Ubd) is a susceptibility gene for virus-triggered autoimmune diabetes in rats.

机构信息

Department of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, USA.

Department of Medicine/Endocrinology, University of Massachusetts Medical School, Worcester, MA, USA.

出版信息

Genes Immun. 2014 Apr-May;15(3):168-75. doi: 10.1038/gene.2013.72. Epub 2014 Jan 23.

Abstract

Genetic studies of type 1 diabetes (T1D) have been advanced by comparative analysis of multiple susceptible and resistant rat strains with a permissive class II MHC haplotype, RT1(u). LEW.1WR1 (but not resistant LEW.1W or WF) rats are susceptible to T1D induced by a TLR3 agonist polyinosinic:polycytidylic acid followed by infection with parvovirus. We have mapped genetic loci for virus-induced T1D susceptibility, identifying a major susceptibility locus (Iddm37) near the MHC. The Iddm37 homologs on mouse and human chromosomes are also diabetes linked. We report that a major effect gene within Iddm37 is diubiquitin (Ubd). Gene expression profiling of pancreatic lymph nodes in susceptible and resistant rats during disease induction showed differences in Ubd transcript abundance. The LEW.1WR1 Ubd promoter allele leads to higher inducible levels of UBD than that of LEW.1W or WF. Using zinc-finger nucleases , we deleted a segment of the LEW.1WR1 Ubd gene and eliminated its expression. UBD-deficient rats show substantially reduced diabetes after viral infection. Complementary studies show that there may be another diabetes gene in addition to Ubd in the Iddm37 interval. These data prove that Ubd is a diabetes susceptibility gene, providing insight into the interplay of multiple genes and environmental factors in T1D susceptibility.

摘要

1 型糖尿病(T1D)的遗传研究通过对具有允许性 II 类 MHC 单倍型 RT1(u)的多种易感和抗性大鼠品系的比较分析得到了推进。LEW.1WR1(而非抗性 LEW.1W 或 WF)大鼠易患 TLR3 激动剂聚肌苷酸:聚胞苷酸诱导的 T1D,随后感染细小病毒。我们已经定位了病毒诱导的 T1D 易感性的遗传位点,在 MHC 附近确定了一个主要的易感性位点(Iddm37)。Iddm37 在小鼠和人类染色体上的同源物也与糖尿病有关。我们报告说,Iddm37 内的一个主要效应基因是二泛素(Ubd)。易感和抗性大鼠在疾病诱导过程中胰腺淋巴结的基因表达谱显示 Ubd 转录物丰度存在差异。LEW.1WR1 Ubd 启动子等位基因导致 UBD 的诱导水平高于 LEW.1W 或 WF。使用锌指核酸酶,我们删除了 LEW.1WR1 Ubd 基因的一段并消除了其表达。UBD 缺陷大鼠在病毒感染后糖尿病明显减少。补充研究表明,除了 Ubd 之外,Iddm37 区间可能还有另一个糖尿病基因。这些数据证明 Ubd 是一个糖尿病易感基因,为 T1D 易感性中多个基因和环境因素的相互作用提供了深入了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/952f/4260472/8789b3ec72f4/nihms550442f1.jpg

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